Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009164961

FEI Number

3009164961

Entity Name

COMPRESSION WORKS INC.

City/State/Country

Birmingham, AL, US

Establishment Address

1634-A Montgomery Hwy, #115, Birmingham, AL 35216, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Complaint File Establishment per 21 CFR 820.198

Owner / Operator

Compression Works Inc. (Owner Number: 10080111)

Owner / Operator Contact Address

1634-A Montgomery Hwy, #115, Birmingham, AL 35216, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K221661

PMA Number

N/A

All Registered Proprietary Names

Abdominal Aortic and Junctional Tourniquet - Stabilized (AAJT-S)

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DXC	Clamp, Vascular	Cardiovascular	Class 2	870.4450	2023-03-11

Official Correspondent

Trey Thorsen

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Compression Works Inc.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009164961. Last updated year: 2026. Please use registration number 3009164961 when referencing this establishment in official correspondence.